3-fluoro-4-(trifluoromethoxy)aniline


Chemical Name: 3-fluoro-4-(trifluoromethoxy)aniline
CAS Number: 1017779-69-9
Product Number: AG0005HA(AGN-PC-02DC4A)
Synonyms:
MDL No:
Molecular Formula: C7H5F4NO
Molecular Weight: 195.1143

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
1.4505
Computed Properties
Molecular Weight:
195.117g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
195.031g/mol
Monoisotopic Mass:
195.031g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



3-Fluoro-4-(trifluoromethoxy)benzenamine, commonly referred to as $name$, is a valuable chemical compound employed in various chemical synthesis processes. This compound plays a crucial role as a building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique molecular structure, characterized by the presence of fluorine atoms, imparts specific properties that make it desirable for use in organic synthesis.One significant application of 3-Fluoro-4-(trifluoromethoxy)benzenamine is in the development of novel pharmaceutical compounds. The introduction of the fluoro and trifluoromethoxy groups in the benzene ring can lead to enhanced biological activity and metabolic stability of the resulting molecules. This property makes $name$ an important intermediate in the synthesis of potential drug candidates, especially in the field of medicinal chemistry.Furthermore, this compound is utilized in the preparation of specialty chemicals and advanced materials. The presence of the fluorine substituents can modify the reactivity and properties of the molecule, allowing for targeted modifications in the desired products. 3-Fluoro-4-(trifluoromethoxy)benzenamine serves as a versatile building block for the creation of functionalized aromatics and heterocycles, which find application in materials science, as well as in the production of agrochemicals with improved efficacy.Overall, the strategic incorporation of 3-Fluoro-4-(trifluoromethoxy)benzenamine in chemical synthesis enables the efficient generation of diverse compounds with tailored properties for applications in pharmaceuticals, specialty chemicals, and materials research.